VALIDATION IMAGES
Lane 1: Rat Heart; Lane 2: Human Liver; Lane 3: Human Kidney; Probed with CYP27A1 (12A4) Monoclonal Antibody (bsm-54432R) at 1:500, overnight at 4°C followed by a conjugated secondary antibody for 60 minutes at 37°C.
IF(ICC) staining with CYP27A1 (12A4) Monoclonal Antibody (bsm-54432R) at 1:100 in HepG2 cells (green). The nuclear counterstain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilized with 0.25% Triton X100/PBS.
IF(ICC) staining with CYP27A1 (12A4) Monoclonal Antibody (bsm-54432R) at 1:100 in LOVO cells (green). The nuclear counterstain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilized with 0.25% Triton X100/PBS.
Paraformaldehyde-fixed and paraffin-embedded Human Liver Cancer tissue incubated with CYP27A1 (12A4) Monoclonal Antibody (bsm-54432R) at 1:100, overnight at 4°C, followed by a conjugated secondary antibody and DAB staining. Counterstained with hematoxylin.
Paraformaldehyde-fixed and paraffin-embedded Human Kidney tissue incubated with CYP27A1 (12A4) Monoclonal Antibody (bsm-54432R) at 1:100, overnight at 4°C, followed by a conjugated secondary antibody and DAB staining. Counterstained with hematoxylin.
Paraformaldehyde-fixed and paraffin-embedded Human Small Intestine tissue incubated with CYP27A1 (12A4) Monoclonal Antibody (bsm-54432R) at 1:100, overnight at 4°C, followed by a conjugated secondary antibody and DAB staining. Counterstained with hematoxylin.
Flow cytometric analysis of HepG2 cells with CYP27A1 (12A4) Monoclonal Antibody (bsm-54432R) at a 1:100 dilution (purple) compared with an unlabeled control (cells without incubation with primary antibody; yellow).